Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays
In many cases, crucial genes show relatively slight changes between groups of samples (e.g. normal vs. disease), and many genes selected from microarray differential analysis by measuring the expression level statistically are also poorly annotated and lack of biological significance. In this paper,...
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2012-06-01
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doaj-e5073047ccb748509604b1508ed1ea092021-09-06T19:40:31ZengDe GruyterJournal of Integrative Bioinformatics1613-45162012-06-019211312510.1515/jib-2012-213biecoll-jib-2012-213Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from MicroarraysWu Xiaogang0Reinhard Christoph1Li Shuyu D.2Huang Hui3Wei Tao4Pandey Ragini5Chen Jake Y.6School of Informatics, Indiana University, Indianapolis, IN 46202, USA United States of AmericaEli Lilly and Company, Indianapolis, IN 46285, United States of AmericaEli Lilly and Company, Indianapolis, IN 46285, United States of AmericaSchool of Informatics, Indiana University, Indianapolis, IN 46202, United States of AmericaEli Lilly and Company, Indianapolis, IN 46285, United States of AmericaMedeoLinx, LLC, Indianapolis, IN 46280, United States of AmericaSchool of Informatics, Indiana University, Indianapolis, IN 46202, USA United States of AmericaIn many cases, crucial genes show relatively slight changes between groups of samples (e.g. normal vs. disease), and many genes selected from microarray differential analysis by measuring the expression level statistically are also poorly annotated and lack of biological significance. In this paper, we present an innovative approach - network expansion and pathway enrichment analysis (NEPEA) for integrative microarray analysis. We assume that organized knowledge will help microarray data analysis in significant ways, and the organized knowledge could be represented as molecular interaction networks or biological pathways. Based on this hypothesis, we develop the NEPEA framework based on network expansion from the human annotated and predicted protein interaction (HAPPI) database, and pathway enrichment from the human pathway database (HPD). We use a recently-published microarray dataset (GSE24215) related to insulin resistance and type 2 diabetes (T2D) as case study, since this study provided a thorough experimental validation for both genes and pathways identified computationally from classical microarray analysis and pathway analysis. We perform our NEPEA analysis for this dataset based on the results from the classical microarray analysis to identify biologically significant genes and pathways. Our findings are not only consistent with the original findings mostly, but also obtained more supports from other literatures.https://doi.org/10.1515/jib-2012-213 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wu Xiaogang Reinhard Christoph Li Shuyu D. Huang Hui Wei Tao Pandey Ragini Chen Jake Y. |
spellingShingle |
Wu Xiaogang Reinhard Christoph Li Shuyu D. Huang Hui Wei Tao Pandey Ragini Chen Jake Y. Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays Journal of Integrative Bioinformatics |
author_facet |
Wu Xiaogang Reinhard Christoph Li Shuyu D. Huang Hui Wei Tao Pandey Ragini Chen Jake Y. |
author_sort |
Wu Xiaogang |
title |
Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays |
title_short |
Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays |
title_full |
Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays |
title_fullStr |
Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays |
title_full_unstemmed |
Network Expansion and Pathway Enrichment Analysis towards Biologically Significant Findings from Microarrays |
title_sort |
network expansion and pathway enrichment analysis towards biologically significant findings from microarrays |
publisher |
De Gruyter |
series |
Journal of Integrative Bioinformatics |
issn |
1613-4516 |
publishDate |
2012-06-01 |
description |
In many cases, crucial genes show relatively slight changes between groups of samples (e.g. normal vs. disease), and many genes selected from microarray differential analysis by measuring the expression level statistically are also poorly annotated and lack of biological significance. In this paper, we present an innovative approach - network expansion and pathway enrichment analysis (NEPEA) for integrative microarray analysis. We assume that organized knowledge will help microarray data analysis in significant ways, and the organized knowledge could be represented as molecular interaction networks or biological pathways. Based on this hypothesis, we develop the NEPEA framework based on network expansion from the human annotated and predicted protein interaction (HAPPI) database, and pathway enrichment from the human pathway database (HPD). We use a recently-published microarray dataset (GSE24215) related to insulin resistance and type 2 diabetes (T2D) as case study, since this study provided a thorough experimental validation for both genes and pathways identified computationally from classical microarray analysis and pathway analysis. We perform our NEPEA analysis for this dataset based on the results from the classical microarray analysis to identify biologically significant genes and pathways. Our findings are not only consistent with the original findings mostly, but also obtained more supports from other literatures. |
url |
https://doi.org/10.1515/jib-2012-213 |
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